FDA Adverse Event Malfunction Summary report: N

MICROLAB AT PLUS 2

MDR report key: 717432 · Received August 15, 2005

Report

Report Number
2915796-2005-00006
Event Type
Malfunction
Date Received
August 15, 2005
Date of Event
July 13, 2005
Report Date
August 11, 2005
Manufacturer
HAMILTON BONADUZ AG
Product Code
JTC
Removal / Correction Number
NA
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
AL, US
Reporter Occupation
OTHER

Narratives

Description of Event or Problem · 1

HAMILTON CO WAS INFORMED IN 7/05 OF AN EVENT THAT OCCURRED IN 05 IN WHICH THE HAMILTON MICROLAB AT +2 INSTRUMENT REPORTEDLY MISPIPETTED SAMPLES. NO DEATH OR INJURY RESULTED FROM THIS EVENT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 MICROLAB AT PLUS 2 MICROTITER DILUTING/DISPENSING JTC HAMILTON BONADUZ AG NA NA

Patients

Seq Age Sex Outcome Treatment
1 NA Other